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Molecular Mechanisms of Endothelial NO Synthase Uncoupling

[ Vol. 20 , Issue. 22 ]

Author(s):

Suxin Luo, Han Lei, Honghua Qin and Yong Xia   Pages 3548 - 3553 ( 6 )

Abstract:


Nitric oxide (NO) is a gaseous signaling molecule and effector in various biological processes. In mammalian cells, NO is produced by a family of NO synthases (NOS). Three NOS isoforms have been identified as: neuronal NOS (nNOS), inducible NOS (iNOS), and endothelial NOS (eNOS). In addition to NO, NOS also produces superoxide anion. This phenomenon is named NOS uncoupling as superoxide generation mainly occurs when NOS is not coupled with its cofactor or substrate. nNOS was first found to produce superoxide under L-arginine depletion condition. Further studies demonstrated that superoxide production is a general feature of all three NOS isoforms. In particular, superoxide generated from uncoupled eNOS has been found to play critical roles in the process of various cardiovascular diseases. Although NOS was first found to produce superoxide only when uncoupled with its cofactor or substrate, recent studies reveal that oxygen reduction to superoxide is an intrinsic process amid NO synthesis. Tetrahydrobiopterin plays a controlling role in preventing superoxide release from the eNOS oxygenase domain. Besides tetrahydrobiopterin, the regulation of eNOS uncoupling by the interactions with other proteins, protein phosphorylation, S-glutathionylation, and endogenous L-arginine derivatives, will be discussed in this review.

Keywords:

NO, endothelial NO synthase, superoxide, tetrahydrobiopterin, uncoupling.

Affiliation:

394 Biomedical Research Tower, Davis Heart and Lung Research Institute, The Ohio State University 460 West 12th Avenue, Columbus, OH 43210 USA.



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